US4617139A - Detergent compositions containing polymers - Google Patents
Detergent compositions containing polymers Download PDFInfo
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- US4617139A US4617139A US06/789,588 US78958885A US4617139A US 4617139 A US4617139 A US 4617139A US 78958885 A US78958885 A US 78958885A US 4617139 A US4617139 A US 4617139A
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- polymer
- radical
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- general formula
- detergent composition
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- 239000000203 mixture Substances 0.000 title claims abstract description 82
- 229920000642 polymer Polymers 0.000 title claims abstract description 73
- 239000003599 detergent Substances 0.000 title claims abstract description 36
- 150000001875 compounds Chemical class 0.000 claims abstract description 21
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 12
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 5
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 4
- 150000008064 anhydrides Chemical class 0.000 claims abstract description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
- -1 alkyl radical Chemical class 0.000 claims description 15
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 14
- 239000002736 nonionic surfactant Substances 0.000 claims description 9
- 125000000129 anionic group Chemical group 0.000 claims description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 5
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 3
- 239000003945 anionic surfactant Substances 0.000 claims description 3
- 239000003093 cationic surfactant Substances 0.000 claims description 2
- 125000004437 phosphorous atom Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 150000002431 hydrogen Chemical class 0.000 claims 3
- ORTFAQDWJHRMNX-UHFFFAOYSA-M oxidooxomethyl Chemical compound [O-][C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-M 0.000 claims 3
- 150000003254 radicals Chemical class 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 101150108015 STR6 gene Proteins 0.000 claims 1
- 150000005840 aryl radicals Chemical class 0.000 claims 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 claims 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 12
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract description 4
- 125000000217 alkyl group Chemical group 0.000 abstract description 4
- 239000000178 monomer Substances 0.000 abstract description 4
- 239000011574 phosphorus Substances 0.000 abstract description 4
- 125000002877 alkyl aryl group Chemical group 0.000 abstract description 2
- 125000003118 aryl group Chemical group 0.000 abstract description 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract description 2
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 1
- 238000009472 formulation Methods 0.000 description 19
- 239000000843 powder Substances 0.000 description 14
- 229920000742 Cotton Polymers 0.000 description 11
- 238000002474 experimental method Methods 0.000 description 11
- 239000002689 soil Substances 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 9
- 239000004744 fabric Substances 0.000 description 9
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 8
- 244000038022 Chenopodium capitatum Species 0.000 description 7
- 235000004391 Chenopodium capitatum Nutrition 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000004115 Sodium Silicate Substances 0.000 description 6
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 6
- 239000001768 carboxy methyl cellulose Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 238000004453 electron probe microanalysis Methods 0.000 description 5
- UFZOPKFMKMAWLU-UHFFFAOYSA-N ethoxy(methyl)phosphinic acid Chemical compound CCOP(C)(O)=O UFZOPKFMKMAWLU-UHFFFAOYSA-N 0.000 description 5
- 229920000058 polyacrylate Polymers 0.000 description 5
- 229920002125 Sokalan® Polymers 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 229960001922 sodium perborate Drugs 0.000 description 4
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 4
- 229910052911 sodium silicate Inorganic materials 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- 238000001694 spray drying Methods 0.000 description 4
- 235000003276 Apios tuberosa Nutrition 0.000 description 3
- 244000105624 Arachis hypogaea Species 0.000 description 3
- 235000010777 Arachis hypogaea Nutrition 0.000 description 3
- 235000010744 Arachis villosulicarpa Nutrition 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 239000004006 olive oil Substances 0.000 description 3
- 235000008390 olive oil Nutrition 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 229910000503 Na-aluminosilicate Inorganic materials 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- 238000004380 ashing Methods 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000007844 bleaching agent Substances 0.000 description 2
- 238000005341 cation exchange Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 229940088598 enzyme Drugs 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000429 sodium aluminium silicate Substances 0.000 description 2
- 235000012217 sodium aluminium silicate Nutrition 0.000 description 2
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
- 235000019351 sodium silicates Nutrition 0.000 description 2
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- YRIZYWQGELRKNT-UHFFFAOYSA-N 1,3,5-trichloro-1,3,5-triazinane-2,4,6-trione Chemical compound ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O YRIZYWQGELRKNT-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 229940025131 amylases Drugs 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- YPQBHUDKOKUINZ-OLXYHTOASA-L bismuth;sodium;(2r,3r)-2,3-dioxidobutanedioate Chemical compound [Na+].[Bi+3].[O-]C(=O)[C@H]([O-])[C@@H]([O-])C([O-])=O YPQBHUDKOKUINZ-OLXYHTOASA-L 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000010612 desalination reaction Methods 0.000 description 1
- CEJLBZWIKQJOAT-UHFFFAOYSA-N dichloroisocyanuric acid Chemical class ClN1C(=O)NC(=O)N(Cl)C1=O CEJLBZWIKQJOAT-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- IILQHMMTOSAJAR-UHFFFAOYSA-L disodium;2-(carboxylatomethoxy)acetate Chemical compound [Na+].[Na+].[O-]C(=O)COCC([O-])=O IILQHMMTOSAJAR-UHFFFAOYSA-L 0.000 description 1
- BNVZBQVIMPLFNA-UHFFFAOYSA-L disodium;2-(carboxymethoxy)butanedioate Chemical compound [Na+].[Na+].OC(=O)COC(C([O-])=O)CC([O-])=O BNVZBQVIMPLFNA-UHFFFAOYSA-L 0.000 description 1
- NPCCEUVRYRJOLM-UHFFFAOYSA-L disodium;2-(carboxymethoxy)propanedioate Chemical compound [Na+].[Na+].OC(=O)COC(C([O-])=O)C([O-])=O NPCCEUVRYRJOLM-UHFFFAOYSA-L 0.000 description 1
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- GQZXNSPRSGFJLY-UHFFFAOYSA-N hydroxyphosphanone Chemical compound OP=O GQZXNSPRSGFJLY-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002455 scale inhibitor Substances 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 230000009291 secondary effect Effects 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- DZCAZXAJPZCSCU-UHFFFAOYSA-K sodium nitrilotriacetate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O DZCAZXAJPZCSCU-UHFFFAOYSA-K 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229950009390 symclosene Drugs 0.000 description 1
- FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 description 1
- 150000004685 tetrahydrates Chemical class 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical class OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3784—(Co)polymerised monomers containing phosphorus
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0036—Soil deposition preventing compositions; Antiredeposition agents
Definitions
- This invention relates to detergent compositions containing polymers and more particularly to fabric-washing detergent compositions containing small amounts of organic polymers for prevention of redeposition of soil.
- the new group of polymers have useful anti-redeposition effects and reduce fabric ashing when used in fabric-washing detergent compositions.
- the new group of polymers has the further advantage that it can aid in the structuring of detergent powder compositions and the dispersibility thereof.
- the present invention provides a detergent composition
- a detergent composition comprising a detergent-active compound and an anti-redeposition polymer formed by reacting:
- R may be a hydrogen atom, a carboxyl residue or, together with the carboxyl group on the adjacent carbon atom, may be an anhydride.
- R' may be a hydrogen atom or a methyl or ethyl residue
- R may be a hydrogen atom, a straight- or branched-chain alkyl residue having from 1 to 18 carbon atoms, a cycloalkyl residue having from 5-12 carbon atoms, an aryl group, an alkaryl group or a radical of the general formula OX, wherein X may be a hydrogen atom or a straight- or branched-chain alkyl group having from 1 to 4 carbon atoms, and
- R'" is a radical of the general formula OX wherein X has the significance defined above.
- R" is a hydrogen atom, a mixture of a polymer of the above formula and one of the general formula: ##STR4## wherein R, R' and R'" have their previous significance, and m and n are integers.
- the carboxyl group in the above formulae may also possibly be bound to the C atom adjacent to the P atom.
- each of R, R' and R" represent hydrogen atoms and R'" represents OH.
- the polymers may be added to compositions either in the acid form or in the form of a salt such as sodium salt.
- a salt such as sodium salt.
- the preponderance of sodium ion in detergent compositions is such that in use the polymer will inevitably be present as the sodium salt.
- the polymers of the invention may be incorporated in detergent compositions either by admixing them with other components of the aqueous crutcher slurry and spray-drying or by adding them to the composition after the spray-drying step with heat-sensitive components such as sodium perborate.
- the amount of the polymer to be incorporated into a detergent composition to obtain anti-redeposition effects will be from 0.1 to 10%, preferably 0.5 to 3% by weight of the composition.
- the polymers may also be incorporated in liquid detergent compositions.
- the precise chemical nature of the detergent compositions into which the polymers are incorporated is not especially critical, since the anti-redeposition effect in a general one.
- the compositions will always contain a detergent-active substance and normally a detergency builder compound too. The remaining components will depend upon whether the composition is a liquid or a powder.
- the amount of detergent-active compound present in the composition will normally be in the range of about 3 to 50% by weight, though higher amounts may also be possible if the composition is presented in the form of a non-aqueous liquid detergent composition.
- the present invention is, however, of particular benefit to detergent compositions having a reduced phosphate builder content, e.g. up to 25%, particularly less than 20% by weight of sodium tripolyphosphate.
- the detergent composition is a powder
- the polymer added to the aqueous detergent slurry before spray-drying will also act as a structurant, which is important in cases wherein sodium tripolyphosphate and/or sodium silicate is present at inadequate levels for proper structuring.
- the detergency builder compound is absent, since large quantities of inorganic materials can lead to physical destabilisation.
- Such compositions will normally contain anionic and nonionic surfactants, possibly a hydrotrope or cosolubiliser and minor components such as antioxidants, fluorescers, colourants and perfumes.
- detergency builders into liquid compositions if care is taken with solubility properties. It may be necessary in some instances to use the more soluble salts such as potassium and triethanolammonium salts for example.
- the builder compound may be either dissolved in the liquid medium or, if the medium is structured, suspended in it.
- the detergent composition When the detergent composition is a powder it will normally be formulated in the conventional two-part form, a first part, which is produced by spray-drying, consisting of anionic and any nonionic and/or cationic surfactants, the detergency builder, sodium silicate as a powder structurant and corrosion inhibitor and the heat-stable minor components such as anti-redeposition agents, including the polymers suggested in this invention, anti-oxidants and fluorescers.
- a first part which is produced by spray-drying, consisting of anionic and any nonionic and/or cationic surfactants, the detergency builder, sodium silicate as a powder structurant and corrosion inhibitor and the heat-stable minor components such as anti-redeposition agents, including the polymers suggested in this invention, anti-oxidants and fluorescers.
- heat-stable compounds such as oxygen bleaches (sodium perborate mono- and/or tetrahydrates, and sodium percarbonate), bleach precursors such as tetra-acetylethylenediamine and sodium nonanoyloxybenzene sulphone, enzymes and perfumes are admixed with the spray-dried part to form a single homogeneous powdered composition.
- oxygen bleaches sodium perborate mono- and/or tetrahydrates, and sodium percarbonate
- bleach precursors such as tetra-acetylethylenediamine and sodium nonanoyloxybenzene sulphone
- enzymes and perfumes are admixed with the spray-dried part to form a single homogeneous powdered composition.
- the nature of the anionic detergent-active compound used in the compositions of the invention is not critical.
- the compound can be any surface-active material which is suitable for use in detergent formulations. Examples of such materials are primary and secondary alkyl sulphate salts, secondary alkane sulphonate salts, olefin sulphonate salts and alkylaryl sulphonate salts, especially the sodium salts of these compounds, and soaps, that is to say salts of fatty acids derived from naturally-occurring materials.
- the anionic detergent-active compound will normally be present in the detergent compositions of the invention in an amount of from about 3-30% by weight of the composition, desirably about 5-15% by weight. Compositions containing more than about 30% by weight of anionic detergent-active component are difficult to process and are also too costly to be commercially viable.
- compositions of the invention may also contain a nonionic surfactant and usually will do so.
- the nonionic surfactants which are preferred for reasons of cost-effectiveness and environmental safety are the ethoxylated alcohols, although other nonionic surfactants such as long-chain alkanolamides may also be used.
- Preferred alcohol ethoxylates are the C 6 -C 22 primary and secondary alcohols ethoxylated with from 5 to 25 moles of ethylene oxide per mole of alcohol.
- Nonionic surfactants may be present in the compositions in amounts of from about 3 to about 20% by weight when present alone to about 1 to about 15% by weight when in the presence of anionic surfactants.
- compositions contain a detergency builder it is preferred that it should be a carbonate, especially sodium carbonate, or an orthophosphate, a pyrophosphate, a tripolyphosphate or a mixture thereof.
- Particularly preferred phosphate builders are a mixture of sodium tripolyphosphate and sodium orthophosphate.
- other organic or inorganic precipitant or sequestrant builders may be used either alone, or in admixture and either with or without phosphate builders.
- alkali metal amine carboxylates such as sodium nitrilotriacetate and sodium ethylenediamine tetraacetate
- alkali metal ether carboxylates such as sodium oxydiacetate, sodium carboxymethyloxysuccinate, sodium carboxymethyloxymalonate and homologues thereof
- alkali metal citrates alkali metal mellitates and salts of polymeric carboxylic acids, such as sodium polymaleate, copolyethylenemaleate, polyitaconate and polyacrylate.
- sodium carbonate is used as a detergency builder, it is advantageous to have present some calcium carbonate having a surface area of at least about 10 m 2 /g, as described in U.K. Pat. No. 1 437 950.
- detergency builder which can be used, either alone or in admixture with other builders, is a cation exchange material, especially a sodium alumino-silicate such as described in U.K. Pat. No 1 429 143 or in Netherlands Patent Application No. 7403381.
- Preferred materials of this type have the formula:
- Such sodium aluminosilicate materials should, of course, be very finely divided so as to minimise deposition on the fabrics during washing.
- water-insoluble aluminosilicate cation-exchange materials such as zeolites
- sodium silicate as corrosion inhibitor and/or structurant
- the alkali metal silicate level in such formulations is normally kept at below a certain level, i.e. not more than about 4% by weight. This will have the consequence that the level of sodium silicate becomes inadequate to provide proper structuring of the powder.
- the use of the polymers according to the invention can also help to compensate the reduced silicate level as a structuring aid.
- the present invention is therefore also of particular benefit as anti-redeposition aid in powder compositions containing less than about 4% by weight of alkali metal silicate materials.
- the total amount of the detergency builder which is used in the composition as a whole is normally from about 10% up to about 60% by weight of the composition, preferably about 15% to about 50%, and the ratio by weight of the detergency builders to the detergent-active compounds which are used is generally from about 3:1 to about 1:2 parts by weight.
- the detergent compositions of the invention may also include any of the conventional optional additives in addition to those already mentioned in the amounts usually employed in detergent compositions.
- these additives include lather controllers, polymers other than the present polymers, including the well-known homopolymers of acrylic acid or its salts, chlorine-releasing bleaching agents such as trichloroisocyanuric acid and alkali metal salts of dichloroisocyanuric acid, fabric-softening agents such as quaternary ammonium salts, anti-ashing aids, starches, inorganic salts such as sodium silicates and sodium sulphate and, usually present in very minor amounts, fluorescent agents, perfurmes, enzymes such as proteases and amylases, germicides and colourants.
- lather controllers polymers other than the present polymers, including the well-known homopolymers of acrylic acid or its salts, chlorine-releasing bleaching agents such as trichloroisocyanuric acid and alkali metal salts of dichloroiso
- the detergent compositions usually have an alkaline pH, generally in the region of pH 9-11, which is achieved by the presence of alkaline salts, especially sodium silicates such as the meta-, neutral or alkaline silicates, preferably at levels up to about 15% by weight.
- alkaline salts especially sodium silicates such as the meta-, neutral or alkaline silicates
- Table 3 below ranks the order of effectiveness of the polymers, the most effective first, after 3, 6 and 9 washes.
- the indication > signifies that the polymers on the left are much better than those on the right.
- Rinse time two 1-minute rinses
- polymer (a) used according to the invention is the most effective as compared with polymer (b)--a polyacrylate--and polymer (c)--an acrylic acid/maleic acid copolymer.
- Rinse time 2 ⁇ 1-minute rinses
- Soil cloth EMPA 101 (Indian ink/olive oil)
- Redeposition monitor combined white cotton
- the detergent powder composition was basically the same as that used in Example I, wherein the level of polymer (in the present case dry acrylic acid/hypophosphorous acid copolymer of ratio 25:1) was varied from 0 to 1.4% by weight, which was compensated by the sodium sulphate level.
- the level of polymer in the present case dry acrylic acid/hypophosphorous acid copolymer of ratio 25:1
- Redeposition monitor combed white cotton
- Polymer (a) of Example II (MW 6200) was compared with a polyacrylate of approximately the same molecular weight (MW 6100) in a base product formulation of Example II containing 23% of sodium tripolyphosphate.
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Abstract
A detergent composition comprising a detergent-active compound and an anti-redeposition polymer formed by reacting
(1) an ethylenic compound of the general formula:
CHR═CR'CO.sub.2 H
in which
R may be a hydrogen atom, a carboxyl residue or, together with the carboxyl group on the adjacent carbon atom, may be an anhydride,
R' may be a hydrogen atom or a methyl or ethyl residue, with
a reducing phosphorus-containing compound of the general formula: ##STR1## in which R" may be a hydrogen atom, a straight- or branched-chain alkyl residue having from 1 to 18 carbon atoms, a cycloalkyl residue having from 5-12 carbon atoms, an aryl group, an alkaryl group or a radical of the general formula OX, wherein X may be a hydrogen atom or a straight- or branched-chain alkyl group having from 1 to 4 carbon atoms, and
R'" is a radical of the general formula OX wherein X has the significance defined above.
The polymer or mixtures of polymers useful in the detergent composition as an anti-redeposition aid have a ratio of acrylic acid or equivalent monomer, i.e. ethylenic compound monomer, to reducing phosphorus-containing compound of from 10:1 to 60:1, preferably from 12:1 to 35:1.
Description
This invention relates to detergent compositions containing polymers and more particularly to fabric-washing detergent compositions containing small amounts of organic polymers for prevention of redeposition of soil.
Redeposition of soil removed from washed articles back onto the articles themselves is a well-known problem which is of particular significance with fabrics articles, and many solutions have been suggested to it. Classically, sodium carboxymethylcellulose was incorporated into fabric-washing compositions, and that compound is still used to-day. More recently, copolymers of ethylene or vinyl methyl ether and maleic anhydride, copolymers of acrylic acid and maleic anhydride and homopolymers of acrylic acid have been suggested in the patent literature (see Procter and Gamble's GB No. 1 269 848 and Unilever's GB No. 1 460 893) and used to some considerable extent in practice.
We have now discovered that a new group of polymers have useful anti-redeposition effects and reduce fabric ashing when used in fabric-washing detergent compositions. The new group of polymers has the further advantage that it can aid in the structuring of detergent powder compositions and the dispersibility thereof.
Accordingly, the present invention provides a detergent composition comprising a detergent-active compound and an anti-redeposition polymer formed by reacting:
an ethylenic compound of the general formula:
CHR═CR'CO.sub.2 H
in which
R may be a hydrogen atom, a carboxyl residue or, together with the carboxyl group on the adjacent carbon atom, may be an anhydride.
R' may be a hydrogen atom or a methyl or ethyl residue, with
a reducing phosphorus-containing compound of the general formula: ##STR2## in which R" may be a hydrogen atom, a straight- or branched-chain alkyl residue having from 1 to 18 carbon atoms, a cycloalkyl residue having from 5-12 carbon atoms, an aryl group, an alkaryl group or a radical of the general formula OX, wherein X may be a hydrogen atom or a straight- or branched-chain alkyl group having from 1 to 4 carbon atoms, and
R'" is a radical of the general formula OX wherein X has the significance defined above.
The polymers formed by this reaction are thought to have the general formula: ##STR3## when R" is other than a hydrogen atom; and where
R" is a hydrogen atom, a mixture of a polymer of the above formula and one of the general formula: ##STR4## wherein R, R' and R'" have their previous significance, and m and n are integers.
Alternatively, the carboxyl group in the above formulae may also possibly be bound to the C atom adjacent to the P atom.
Polymers of the type described are disclosed in British Pat. Nos. 1 458 235 and 1 595 688 (Ciba-Geigy), where they are suggested as scale-inhibitors for use in industrial situations, e.g. industrial boilers, steam power plants, cooling water systems and water desalination. However, it has been discovered that only a limited range of the disclosed polymers is suitable for use in detergent compositions as an effective anti-redeposition aid for improving the whiteness or brightness retention of fabrics. That range is where the ratio of acrylic acid or equivalent monomer, i.e. ethylene compound monomer, to reducing phosphorus-containing compound is from 10:1 to 60:1, preferably from 12:1 to 35:1; polymers outside this range and particularly having the ratio below 10:1 being much less effective anti-redeposition agents.
Preferably, each of R, R' and R" represent hydrogen atoms and R'" represents OH. The polymers may be added to compositions either in the acid form or in the form of a salt such as sodium salt. However, the preponderance of sodium ion in detergent compositions is such that in use the polymer will inevitably be present as the sodium salt.
The polymers of the invention may be incorporated in detergent compositions either by admixing them with other components of the aqueous crutcher slurry and spray-drying or by adding them to the composition after the spray-drying step with heat-sensitive components such as sodium perborate.
The amount of the polymer to be incorporated into a detergent composition to obtain anti-redeposition effects will be from 0.1 to 10%, preferably 0.5 to 3% by weight of the composition.
The polymers may also be incorporated in liquid detergent compositions.
The precise chemical nature of the detergent compositions into which the polymers are incorporated is not especially critical, since the anti-redeposition effect in a general one. The compositions will always contain a detergent-active substance and normally a detergency builder compound too. The remaining components will depend upon whether the composition is a liquid or a powder. The amount of detergent-active compound present in the composition will normally be in the range of about 3 to 50% by weight, though higher amounts may also be possible if the composition is presented in the form of a non-aqueous liquid detergent composition.
The present invention is, however, of particular benefit to detergent compositions having a reduced phosphate builder content, e.g. up to 25%, particularly less than 20% by weight of sodium tripolyphosphate. When the detergent composition is a powder, the polymer added to the aqueous detergent slurry before spray-drying will also act as a structurant, which is important in cases wherein sodium tripolyphosphate and/or sodium silicate is present at inadequate levels for proper structuring.
If it is a liquid, it may well be that the detergency builder compound is absent, since large quantities of inorganic materials can lead to physical destabilisation. Such compositions will normally contain anionic and nonionic surfactants, possibly a hydrotrope or cosolubiliser and minor components such as antioxidants, fluorescers, colourants and perfumes. However, it is perfectly feasible to incorporate detergency builders into liquid compositions if care is taken with solubility properties. It may be necessary in some instances to use the more soluble salts such as potassium and triethanolammonium salts for example. The builder compound may be either dissolved in the liquid medium or, if the medium is structured, suspended in it.
When the detergent composition is a powder it will normally be formulated in the conventional two-part form, a first part, which is produced by spray-drying, consisting of anionic and any nonionic and/or cationic surfactants, the detergency builder, sodium silicate as a powder structurant and corrosion inhibitor and the heat-stable minor components such as anti-redeposition agents, including the polymers suggested in this invention, anti-oxidants and fluorescers. Less heat-stable compounds such as oxygen bleaches (sodium perborate mono- and/or tetrahydrates, and sodium percarbonate), bleach precursors such as tetra-acetylethylenediamine and sodium nonanoyloxybenzene sulphone, enzymes and perfumes are admixed with the spray-dried part to form a single homogeneous powdered composition.
The nature of the anionic detergent-active compound used in the compositions of the invention is not critical. The compound can be any surface-active material which is suitable for use in detergent formulations. Examples of such materials are primary and secondary alkyl sulphate salts, secondary alkane sulphonate salts, olefin sulphonate salts and alkylaryl sulphonate salts, especially the sodium salts of these compounds, and soaps, that is to say salts of fatty acids derived from naturally-occurring materials. The anionic detergent-active compound will normally be present in the detergent compositions of the invention in an amount of from about 3-30% by weight of the composition, desirably about 5-15% by weight. Compositions containing more than about 30% by weight of anionic detergent-active component are difficult to process and are also too costly to be commercially viable.
The compositions of the invention may also contain a nonionic surfactant and usually will do so. The nonionic surfactants which are preferred for reasons of cost-effectiveness and environmental safety are the ethoxylated alcohols, although other nonionic surfactants such as long-chain alkanolamides may also be used. Preferred alcohol ethoxylates are the C6 -C22 primary and secondary alcohols ethoxylated with from 5 to 25 moles of ethylene oxide per mole of alcohol. Nonionic surfactants may be present in the compositions in amounts of from about 3 to about 20% by weight when present alone to about 1 to about 15% by weight when in the presence of anionic surfactants.
When the compositions contain a detergency builder it is preferred that it should be a carbonate, especially sodium carbonate, or an orthophosphate, a pyrophosphate, a tripolyphosphate or a mixture thereof. Particularly preferred phosphate builders are a mixture of sodium tripolyphosphate and sodium orthophosphate. However, other organic or inorganic precipitant or sequestrant builders may be used either alone, or in admixture and either with or without phosphate builders. Examples of these are alkali metal amine carboxylates, such as sodium nitrilotriacetate and sodium ethylenediamine tetraacetate, alkali metal ether carboxylates, such as sodium oxydiacetate, sodium carboxymethyloxysuccinate, sodium carboxymethyloxymalonate and homologues thereof, alkali metal citrates, alkali metal mellitates and salts of polymeric carboxylic acids, such as sodium polymaleate, copolyethylenemaleate, polyitaconate and polyacrylate. When sodium carbonate is used as a detergency builder, it is advantageous to have present some calcium carbonate having a surface area of at least about 10 m2 /g, as described in U.K. Pat. No. 1 437 950.
Another type of detergency builder which can be used, either alone or in admixture with other builders, is a cation exchange material, especially a sodium alumino-silicate such as described in U.K. Pat. No 1 429 143 or in Netherlands Patent Application No. 7403381. Preferred materials of this type have the formula:
(Na.sub.2 O).sub.0.7-1.1.Al.sub.2 O.sub.3 (SiO.sub.2).sub.1.3-3.3
and may be amorphous or crystalline, with some bound water usually in an amount of about 10-30% depending on the drying conditions used. Such sodium aluminosilicate materials should, of course, be very finely divided so as to minimise deposition on the fabrics during washing.
Lately there is a growing trend (due to legislation to a number of countries) to reduce the levels of, or replace completely sodium tripolyphosphate in fabric-washing products. One of the consequences of this is a loss of some of the valuable secondary effects of sodium tripolyphosphate, which include control of soil redeposition and fabric ash, powder structuring and powder dispersibility.
All of these can, to a certain degree, be helped by the use of the present polymers.
If water-insoluble aluminosilicate cation-exchange materials, such as zeolites, are used to replace sodium tripolyphosphate wholly or partially, the presence of higher levels of sodium silicate (as corrosion inhibitor and/or structurant) could present problems with respect to the formation of insoluble material being deposited onto the fabrics. In order to overcome this problem the alkali metal silicate level in such formulations is normally kept at below a certain level, i.e. not more than about 4% by weight. This will have the consequence that the level of sodium silicate becomes inadequate to provide proper structuring of the powder. In this case the use of the polymers according to the invention can also help to compensate the reduced silicate level as a structuring aid.
The present invention is therefore also of particular benefit as anti-redeposition aid in powder compositions containing less than about 4% by weight of alkali metal silicate materials.
The total amount of the detergency builder which is used in the composition as a whole is normally from about 10% up to about 60% by weight of the composition, preferably about 15% to about 50%, and the ratio by weight of the detergency builders to the detergent-active compounds which are used is generally from about 3:1 to about 1:2 parts by weight.
The detergent compositions of the invention may also include any of the conventional optional additives in addition to those already mentioned in the amounts usually employed in detergent compositions. Examples of these additives include lather controllers, polymers other than the present polymers, including the well-known homopolymers of acrylic acid or its salts, chlorine-releasing bleaching agents such as trichloroisocyanuric acid and alkali metal salts of dichloroisocyanuric acid, fabric-softening agents such as quaternary ammonium salts, anti-ashing aids, starches, inorganic salts such as sodium silicates and sodium sulphate and, usually present in very minor amounts, fluorescent agents, perfurmes, enzymes such as proteases and amylases, germicides and colourants. The detergent compositions usually have an alkaline pH, generally in the region of pH 9-11, which is achieved by the presence of alkaline salts, especially sodium silicates such as the meta-, neutral or alkaline silicates, preferably at levels up to about 15% by weight.
The invention is illustrated by the following Examples in which parts and percentages are by weight except where otherwise indicated.
In a single experiment, the anti-redeposition effect of three comparable formulations containing different polymers were investigated. First, solutions containing 4 g/liter of the detergent compositions shown below in water of 40° French hardness were prepared.
______________________________________
% by weight
______________________________________
Sodium dodecylbenzene sulphonate
6.0
C.sub.14-15 11 EO nonionic surfactant
2.0
Hardened sodium stearate
3.0
Sodium tripolyphosphate
7.5
Sodium orthophosphate
7.5
Sodium alkaline silicate
7.0
Sodium perborate 20.0
Sodium sulphate 20.0
Sodium carboxymethylcellulose
0.5
Polymer (see Table 1)
1.0
Water up to 100.0
______________________________________
The three formulations tested were derived from the composition shown above by addition of the components shown in Table 1.
TABLE 1
______________________________________
% by weight
Formulation:
Polymer Added A B C
______________________________________
None Nil
Dry acrylic acid/maleic acid copolymer
1
(*Sokalan CP5 ex BASF)
Dry acrylic acid/hypophosphorous acid
1
copolymer (16:1)
(*CHEL 3229 ex Ciba-Geigy)
______________________________________
*Registered Trade Mark
Each of these three compositions was used to wash white cotton monitors in the presence of standard EMPA 101 (Indian ink/olive oil) solid detergency test cloths in Tergotometers®. The was conditions were:
Temperature: 60° C.
Wash time: 20 minutes
Flood time: 5 minutes
Rinse time: 2 1-minute rinses
This wash operation was performed six times and after each wash cycle the change in reflectance of the cotton monitors was measured by standard techniques. The results are shown in Table 2.
TABLE 2
______________________________________
Change in Reflectance of Cotton Monitors (ΔR)
Wash Cycle
Formulation
1 2 3 4 5 6
______________________________________
A 14.6 17.3 18.7 Not measured
21.8 23.0
B 9.0 10.8 12.7 Not measured
16.1 16.5
C 1.9 2.2 3.2 Not measured
4.6 5.3
______________________________________
It can be seen that the change in reflectance of the cotton monitor washed with formulation C, the formulation in accordance with the invention, is lower than either the control formulation A containing no anti-redeposition polymer other than sodium carboxymethyl-cellulose (SCMC), or formulation B containing both SCMC and Sokalan CP5®, which probably represents the best combination presently known to the detergents art.
In multiple Tergotometer® wash experiments the effectiveness of three different polymers in preventing the redeposition of soil resulting from differently soild test cloths and from article pieces (cut from soiled tea towels) was compared, using the following basic detergent powder formulation at a dosage of 4 g/l.
______________________________________
% by weight
______________________________________
Sodium dodecylbenzene sulphonate
9.0
C.sub.13-15 alcohol/7 ethylene oxide
4.0
nonionic surfactant
Sodium tripolyphosphate (STP)
25.0
Sodium carbonate 5.0
Sodium alkaline silicate
6.0
Sodium carboxymethylcellulose
0.5
Sodium sulphate 25.0
Sodium perborate 4 H.sub.2 O (post dosed)
15.0
Polymer* 1.0
Water up to 100.0
______________________________________
% STP breakdown during manufacture 30%.
*Polymer (a) = Dry acrylic acid/hypophosphorous acid copolymer (25:1)
Polymer (b) = Commercial polyacrylate (Natrol ® 34)
Polymer (c) = Dry acrylic acid/maleic acid copolymer (Sokalan ® CP5 e
BASF).
The wash conditions were the same as those used in Example I.
Table 3 below ranks the order of effectiveness of the polymers, the most effective first, after 3, 6 and 9 washes. The indication > signifies that the polymers on the left are much better than those on the right.
TABLE 3
______________________________________
Number of washes
Cloth soiled with:
3 6 9
______________________________________
1. Indian ink/groundnut
b a c -a b c
oil/iron oxide
2. Indian ink/groundnut
c a>b -a>b>c
oil/iron oxide
3. Indian ink/groundnut
-a b c b a c
oil/iron oxide/milk powder
4. EMPA 101 (Indian ink/
-a b>c c b a
olive oil)
5. EMPA 116 (Indian ink/
b a>c -a b c
milk/blood)
6. VCD (Vacuum cleaner
-a>b c -a>b c
dust)
7. Lanolin/kaolin/carbon
-a>b c -a>b c
black/iron oxide)
8. Clay/candy black -a c>b -a c>b
9. Article pieces -a>b>c -a>b>c
-a>b>c
______________________________________
It can be seen that overall the formulation with polymer (a) according to the invention is superior to the other formulations containing polymer (b) or polymer (c).
Another series of experiments was made to compare the anti-redeposition effects of polymer (a), polymer (b) and polymer (c) in the formulation of Example II, using dirty wash liquor as a source of soil. In an attempt to obtain a homogeneous supply of "real" soil, laundry loads were washed in a twin-tub washing machine and the resulting dirty wash liquor was used as a source of soil in subsequent Tergotometer® deposition experiments under the following wash conditions:
Temperature: 60° C.
Wash time: 20 minutes
Flood time: 5 minutes
Rinse time: two 1-minute rinses
Soiled wash liquor adjusted to: 40° French hardness
Polymer added: at 1% of product.
4×2.5 kg soiled loads were washed consecutively for 20 minutes at 80° C. in the same 35 liters of demineralised water with the same base product without polymer to be used in the Tergotometer® experiments at a product dosage of 4 g/l.
The results of the Tergotometer® deposition experiments depicted in Table 4 show changes in Reflectance (-ΔR) of the white cotton monitors:
TABLE 4
______________________________________
(-ΔR)
Without Polymer Polymer
Polymer
Exp. Number of Polymer (a) (b) (c)
N°
Washes 0 0.5% 1% 1% 1%
______________________________________
1 4 3.1 -- 1.7 -- 2.3
8 4.7 -- 2.5 -- 3.6
12 4.9 -- 2.1 -- 4.2
2 4 2.9 -- 2.2 -- 2.4
8 5.1 -- 3.8 -- 4.3
12 6.4 -- 4.6 -- 5.1
3 4 3.3 0.8 0.9 1.3 1.7
8 5.1 2.7 2.1 2.5 3.
______________________________________
Each horizontal line of -ΔR values was obtained from one batch of soiled liquor, a different batch being used for each subsequent set of 4 washes. Comparisons between the effect of various polymers, wash compositions, etc. are only legitimate within one experiment. Comparisons should not be made between different experiments because of the different batches of wash liquor used.
The above data show that polymer (a) used according to the invention is the most effective as compared with polymer (b)--a polyacrylate--and polymer (c)--an acrylic acid/maleic acid copolymer.
A series of Tergotometer® evaluations was carried out to compare the effectiveness of acrylic acid/hypophosphorous acid copolymer (25:1), i.e. polymer (a) of Example II, with that of Sokalan CP5 ex BASF, i.e. polymer (c) of Example II, in a normal anionic/nonionic formulation containing various builder systems.
Wash conditions:
Product dosage: 4 g/l
Temperature: 60° C.
Wash time: 20 minutes
Flood time: 5 minutes
Rinse time: 2×1-minute rinses
Soil cloth: EMPA 101 (Indian ink/olive oil)
Redeposition monitor: combined white cotton
Polymer level
in product: 1%
The change of reflectance of cotton monitors read after 6 washes is shown in the following Table 5.
TABLE 5
______________________________________
Polymer
Builder system in Product
nil (a) (c)
______________________________________
18% sodium tripolyphosphate
9.1 7.7 10.2
13% zeolite A 5.4 4.0 4.1
30% sodium carbonate
B 13.1 7.1 9.1
20% calcite
______________________________________
Again, the above results clearly show that the change in reflectance of the cotton monitors washed with formulations containing polymer (a), the formulation of the invention, is lower than that of the cotton monitors washed with formulations containing polymer (c) outside the invention.
In this Example the effect of polymer level in a detergent powder composition on the redeposition of soil was examined in a Tergotometer® wash experiment.
The detergent powder composition was basically the same as that used in Example I, wherein the level of polymer (in the present case dry acrylic acid/hypophosphorous acid copolymer of ratio 25:1) was varied from 0 to 1.4% by weight, which was compensated by the sodium sulphate level.
Wash conditions:
Temperature: 60° Cl
Wash time: 20 minutes
Flood time: 5 minutes
Rinse time: 2×1 minute
Soil cloth: EMPA 101
Redeposition monitor: combed white cotton
Product dosage: 4 g/l
Water hardness: 40° French hardness
The results are shown in Table 6 below.
TABLE 6
______________________________________
% polymer 0 0.5 0.8 1.1 1.4
______________________________________
ΔR after 3 washes
18.5 11.4 8.0 5.6 5.3
______________________________________
Experiments were conducted on redeposition early in the wash. In the early stages of a wash, product concentrations are low because of the finite rate of solution of product ingredients and because of the mechanical loss of powder in the sump of the washing machine. In the present Tergotometer® experiments 1 g/l of product was used with a polymer content of 3% by weight. This was to simulate the beginning of a wash nominally at 5 g/l (European conditions) with 1% of polymer but when only 1 g/l of product had dissolved together with a higher proportion of the polymer. The wash time was set at 5 minutes.
Polymer (a) of Example II (MW 6200) was compared with a polyacrylate of approximately the same molecular weight (MW 6100) in a base product formulation of Example II containing 23% of sodium tripolyphosphate.
The results are given in the following Table 7, showing change in reflectance (-ΔR) of cotton monitors after 3 washes.
TABLE 7
______________________________________
(-ΔR) after 3 washes
No Polymer + Polymer (a)
+ Polyacrylate
______________________________________
11.9 5.9 7.5
11.6 6.3 7.1
11.2 7.0 8.8
10.7 6.5 8.1
______________________________________
The results again show superiority of the product with polymer (a) of the invention to the product containing polyacrylate outside the invention.
Claims (7)
1. A detergent composition comprising from 3 to 50% by weight of a detergent-active compound selected from the group consisting of anionic, nonionic and cationic surfactants and mixtures thereof, from 0 to 60% by weight of a detergency builder and from 0.1 to 10% by weight of an anti-redeposition polymer, said polymer being one having the general formula: ##STR5## wherein R is a group selected from hydrogen, a carboxyl radical, an anhydride formed from said carboxyl radical and from the carboxyl radical on the adjacent carbon atom in said formula, and combinations thereof;
R' is a group selected from hydrogen, methyl or ethyl radical, and combinations thereof;
R" is a group selected from hydrogen, straight- or branched-chain alkyl radical having from 1 to 18 carbon atoms, cycloalkyl radical having from 5-12 carbon atoms, an aryl radical, an alkaryl radical and a radical of the general formula OX, wherein X may be a hydrogen atom or a straight- or branched-chain alkyl radical having from 1 to 4 carbon atoms;
R'" is a radical of the general formula OX, wherein X is defined as above; and n is an integer, but when R" is hydrogen, then the polymer is a mixture of a polymer of the above formula and one of the general formula: ##STR6## wherein R, R' and R'" have their previous significance, and m and n are integers, such as the ratio of the CHR--CR'(CO2 H) unit to the phosphorus atom is from 10:1 to 60:1.
2. A detergent composition according to claim 1, wherein said ratio is from 12:1 to 35:1.
3. A detergent composition according to claim 1, wherein said anti-redeposition polymer is present in an amount of 0.5 to 3% by weight of the total composition.
4. A detergent composition according to claim 1, which comprises from 10 to 60% by weight of a detergency builder.
5. A detergent composition according to claim 4, which comprises up to 25% by weight of a phosphate builder.
6. A detergent composition according to claim 5, comprising less than 20% by weight of sodium tripolyphosphate.
7. A detergent composition according to claim 1, containing an alkali metal silicate in an amount of less than about 4% by weight of the total composition.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8426737 | 1984-10-23 | ||
| GB848426737A GB8426737D0 (en) | 1984-10-23 | 1984-10-23 | Detergent compositions |
| GB8520184 | 1985-08-12 | ||
| GB858520184A GB8520184D0 (en) | 1985-08-12 | 1985-08-12 | Detergent compositions containing polymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4617139A true US4617139A (en) | 1986-10-14 |
Family
ID=26288362
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/789,588 Expired - Fee Related US4617139A (en) | 1984-08-12 | 1985-10-21 | Detergent compositions containing polymers |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4617139A (en) |
| EP (1) | EP0182411B1 (en) |
| AU (1) | AU600654B2 (en) |
| BR (1) | BR8505272A (en) |
| CA (1) | CA1237041A (en) |
| DE (1) | DE3573611D1 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4900466A (en) * | 1985-11-01 | 1990-02-13 | Lever Brothers Company | Process for preparing needle-shaped crystal growth modified burkeite detergent additive |
| US5409571A (en) * | 1992-08-27 | 1995-04-25 | Hakuto Co., Ltd. | Scale deposit inhibitor for kraft digesters and method for controlling scale deposition in kraft digesters |
| US6034045A (en) * | 1997-02-25 | 2000-03-07 | Church & Dwight Co., Inc. | Liquid laundry detergent composition containing a completely or partially neutralized carboxylic acid-containing polymer |
| WO2003099981A1 (en) * | 2002-05-23 | 2003-12-04 | The Procter & Gamble Company | Methods and articles for reducing airborne particulates |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0664334A1 (en) * | 1994-01-19 | 1995-07-26 | The Procter & Gamble Company | Detergent compositions inhibiting dye transfer |
| DE69819593T2 (en) | 1997-05-09 | 2004-09-16 | Rohm And Haas Co. | Detergent formulations |
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|---|---|---|---|---|
| US2957931A (en) * | 1949-07-28 | 1960-10-25 | Socony Mobil Oil Co Inc | Synthesis of compounds having a carbonphosphorus linkage |
| GB935733A (en) * | 1961-03-16 | 1963-09-04 | Basf Ag | Detergents and cleaning products |
| US3284364A (en) * | 1963-01-25 | 1966-11-08 | American Cyanamid Co | Soil anti-redeposition agents |
| US3558499A (en) * | 1969-07-01 | 1971-01-26 | Atlas Chem Ind | Anti-redeposition agents |
| GB1269848A (en) * | 1968-11-27 | 1972-04-06 | Procter & Gamble | Improved bleaching composition |
| US3684779A (en) * | 1971-04-07 | 1972-08-15 | John N Rapko | Maleic/acrylic/alkenyl phosphonate terpolymers |
| GB1290724A (en) * | 1968-10-05 | 1972-09-27 | ||
| GB1458235A (en) * | 1974-06-11 | 1976-12-08 | Ciba Geigy Uk Ltd | Inhibiting scale formation in aqueous systems |
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| US4105551A (en) * | 1974-06-11 | 1978-08-08 | Ciba Geigy (Uk) Limited | Treatment of aqueous systems |
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| GB1551239A (en) * | 1975-09-21 | 1979-08-30 | Procter & Gamble | Built detergent compositions |
| DE2921374A1 (en) * | 1978-05-26 | 1979-12-06 | Ciba Geigy Uk Ltd | TREATMENT OF AQUATIC SYSTEMS |
| US4372870A (en) * | 1981-07-24 | 1983-02-08 | Betz Laboratories, Inc. | Method and composition for treating aqueous mediums |
| US4563284A (en) * | 1984-08-06 | 1986-01-07 | The B. F. Goodrich Company | Inhibition of salt precipitation in aqueous systems |
-
1985
- 1985-10-18 CA CA000493297A patent/CA1237041A/en not_active Expired
- 1985-10-21 DE DE8585201716T patent/DE3573611D1/en not_active Expired
- 1985-10-21 US US06/789,588 patent/US4617139A/en not_active Expired - Fee Related
- 1985-10-21 EP EP85201716A patent/EP0182411B1/en not_active Expired
- 1985-10-22 BR BR8505272A patent/BR8505272A/en unknown
- 1985-10-23 AU AU48987/85A patent/AU600654B2/en not_active Expired - Fee Related
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| GB1290724A (en) * | 1968-10-05 | 1972-09-27 | ||
| GB1269848A (en) * | 1968-11-27 | 1972-04-06 | Procter & Gamble | Improved bleaching composition |
| US3558499A (en) * | 1969-07-01 | 1971-01-26 | Atlas Chem Ind | Anti-redeposition agents |
| US3684779A (en) * | 1971-04-07 | 1972-08-15 | John N Rapko | Maleic/acrylic/alkenyl phosphonate terpolymers |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4900466A (en) * | 1985-11-01 | 1990-02-13 | Lever Brothers Company | Process for preparing needle-shaped crystal growth modified burkeite detergent additive |
| US5409571A (en) * | 1992-08-27 | 1995-04-25 | Hakuto Co., Ltd. | Scale deposit inhibitor for kraft digesters and method for controlling scale deposition in kraft digesters |
| US6034045A (en) * | 1997-02-25 | 2000-03-07 | Church & Dwight Co., Inc. | Liquid laundry detergent composition containing a completely or partially neutralized carboxylic acid-containing polymer |
| WO2003099981A1 (en) * | 2002-05-23 | 2003-12-04 | The Procter & Gamble Company | Methods and articles for reducing airborne particulates |
| EP2248881A1 (en) * | 2002-05-23 | 2010-11-10 | The Procter and Gamble Company | Methods and articles for reducing airborne particles |
Also Published As
| Publication number | Publication date |
|---|---|
| AU600654B2 (en) | 1990-08-23 |
| BR8505272A (en) | 1986-08-05 |
| EP0182411B1 (en) | 1989-10-11 |
| AU4898785A (en) | 1986-05-01 |
| CA1237041A (en) | 1988-05-24 |
| EP0182411A2 (en) | 1986-05-28 |
| DE3573611D1 (en) | 1989-11-16 |
| EP0182411A3 (en) | 1987-11-25 |
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